Dla naszego klient, międzynarodowej firmy z obszaru badań klinicznych, poszukujemy kandydatów na stanowisko SCRA. Senior Clinical Research AssociateMiejsce pracy: Warszawa Zadania: monitorowanie badań klinicznych na terenie całej Polski, w różnych obszarach terapeutycznych set-up badań
required REQUIREMENTS - Bachelor degree or equivalent within Medicine, Biological Science, Pharmacology, Nursing. - Experience in performing a Clinical Research Associate role - Fluent in English and Dutch (written and spoken) - Willingness and ability to travel
communication, and the need for additional training. REQUIREMENTS - Knowledge of Good Clinical Practice/ICH Guideline - Strong organizational skills - Good computer skills - Fluency in Dutch and English - Bachelor in Life Science Are you interested and
DetailsOur Client is a dynamically growing Contract Research Organization with over 200 employees operating in 16 countries in Europe. Company has nearly 20 years of expertise on the market and provides services to more than 250 clients worldwide. Our Client is passionate about talented people who dream big ...
THE COMPANY Our client is a professional Pharmaceutical organization, based in Netherlands. Our client is a professional Clinical Research organization, based in Utrecht Netherlands. The client is a global CRO that operates in both the pharmaceutical
policy, SOPs and regulatory requirements. May include international and overnight travelling RESPONSIBILITIES - Monitor on-site and remotely clinical trials. - Review and support site staff to maintain Site Master File(SMF). - Update Clinical Trial Management
patient sample receipt - biobanking of immune cells derived from clinical patient material - participate in the maintenance of equipment and lab areas REQUIREMENTS - Bachelor in Laboratory Techniques/Master in Biomedical Sciences or a related field - at least two
Assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. RESPONSIBILITIES - Assisting the clinical team in
mentoring and receive structured quarterly reviews on performance, as well as promotion and bonus awards. ROLE DESCRIPTION Assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining
responsibilities - Reviewing project tasks and timelines and assigning team members - Liaising with other functional managers to ensure consistency within the company REQUIREMENTS - Substantial clinical trials development experience is required - Experience supervising or
THE COMPANY Our client is a professional Healthcare and Pharmaceutical organization, based in Netherlands. The company is a research center that focuses on nutrition and is located in a state of the art Life Science research center ...
you are responsible the maintenance of clinical tracking system and support teams in preparing trial documents, study budgets. REQUIREMENTS - BSc or similar in a scientific discipline - Relevant experience in administrative tasks - Experienced in MS Office ...
ROLE DESCRIPTION The client is looking for a clinical trials coordinator to join its Clinical Department who will manage national and international clinical studies from phase I to phase IV RESPONSIBILITIES - Develop protocol and all other